JP5931051B2 - 置換カルバゾール誘導体および有機エレクトロニクスにおけるその使用 - Google Patents

置換カルバゾール誘導体および有機エレクトロニクスにおけるその使用 Download PDF

Info

Publication number
JP5931051B2
JP5931051B2 JP2013503205A JP2013503205A JP5931051B2 JP 5931051 B2 JP5931051 B2 JP 5931051B2 JP 2013503205 A JP2013503205 A JP 2013503205A JP 2013503205 A JP2013503205 A JP 2013503205A JP 5931051 B2 JP5931051 B2 JP 5931051B2
Authority
JP
Japan
Prior art keywords
group
substituted
unsubstituted
alkyl
aryl
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Active
Application number
JP2013503205A
Other languages
English (en)
Japanese (ja)
Other versions
JP2013528929A5 (fr
JP2013528929A (ja
Inventor
ランガー ニコル
ランガー ニコル
シルトクネヒト クリスティアン
シルトクネヒト クリスティアン
惣一 渡部
惣一 渡部
フックス エヴェリン
フックス エヴェリン
ヴァーゲンブラスト ゲアハート
ヴァーゲンブラスト ゲアハート
レナルツ クリスティアン
レナルツ クリスティアン
モルト オリヴァー
モルト オリヴァー
ドアマン コリンナ
ドアマン コリンナ
アーヴィト フンツェ
フンツェ アーヴィト
ラルフ クラウゼ
クラウゼ ラルフ
シュミート ギュンター
シュミート ギュンター
ホイザー カルステン
ホイザー カルステン
ファン エルスベアゲン フォルカー
ファン エルスベアゲン フォルカー
フリードリヒ ベアナー ヘアバート
フリードリヒ ベアナー ヘアバート
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
BASF SE
Ams Osram International GmbH
Koninklijke Philips NV
Original Assignee
BASF SE
Osram Opto Semiconductors GmbH
Koninklijke Philips NV
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by BASF SE, Osram Opto Semiconductors GmbH, Koninklijke Philips NV filed Critical BASF SE
Publication of JP2013528929A publication Critical patent/JP2013528929A/ja
Publication of JP2013528929A5 publication Critical patent/JP2013528929A5/ja
Application granted granted Critical
Publication of JP5931051B2 publication Critical patent/JP5931051B2/ja
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • HELECTRICITY
    • H10SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10KORGANIC ELECTRIC SOLID-STATE DEVICES
    • H10K85/00Organic materials used in the body or electrodes of devices covered by this subclass
    • H10K85/60Organic compounds having low molecular weight
    • H10K85/649Aromatic compounds comprising a hetero atom
    • H10K85/657Polycyclic condensed heteroaromatic hydrocarbons
    • H10K85/6572Polycyclic condensed heteroaromatic hydrocarbons comprising only nitrogen in the heteroaromatic polycondensed ring system, e.g. phenanthroline or carbazole
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/02Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
    • C07D405/04Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04Ortho-condensed systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D491/00Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
    • C07D491/02Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
    • C07D491/04Ortho-condensed systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D519/00Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F7/00Compounds containing elements of Groups 4 or 14 of the Periodic Table
    • C07F7/02Silicon compounds
    • C07F7/08Compounds having one or more C—Si linkages
    • C07F7/0803Compounds with Si-C or Si-Si linkages
    • C07F7/081Compounds with Si-C or Si-Si linkages comprising at least one atom selected from the elements N, O, halogen, S, Se or Te
    • C07F7/0812Compounds with Si-C or Si-Si linkages comprising at least one atom selected from the elements N, O, halogen, S, Se or Te comprising a heterocyclic ring
    • C07F7/0814Compounds with Si-C or Si-Si linkages comprising at least one atom selected from the elements N, O, halogen, S, Se or Te comprising a heterocyclic ring said ring is substituted at a C ring atom by Si
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F7/00Compounds containing elements of Groups 4 or 14 of the Periodic Table
    • C07F7/02Silicon compounds
    • C07F7/08Compounds having one or more C—Si linkages
    • C07F7/0834Compounds having one or more O-Si linkage
    • C07F7/0838Compounds with one or more Si-O-Si sequences
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F9/00Compounds containing elements of Groups 5 or 15 of the Periodic Table
    • C07F9/02Phosphorus compounds
    • C07F9/547Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
    • C07F9/6564Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms
    • C07F9/6568Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms having phosphorus atoms as the only ring hetero atoms
    • C07F9/65683Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms having phosphorus atoms as the only ring hetero atoms the ring phosphorus atom being part of a phosphine
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09BORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B57/00Other synthetic dyes of known constitution
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K11/00Luminescent, e.g. electroluminescent, chemiluminescent materials
    • C09K11/06Luminescent, e.g. electroluminescent, chemiluminescent materials containing organic luminescent materials
    • HELECTRICITY
    • H05ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
    • H05BELECTRIC HEATING; ELECTRIC LIGHT SOURCES NOT OTHERWISE PROVIDED FOR; CIRCUIT ARRANGEMENTS FOR ELECTRIC LIGHT SOURCES, IN GENERAL
    • H05B33/00Electroluminescent light sources
    • H05B33/10Apparatus or processes specially adapted to the manufacture of electroluminescent light sources
    • HELECTRICITY
    • H05ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
    • H05BELECTRIC HEATING; ELECTRIC LIGHT SOURCES NOT OTHERWISE PROVIDED FOR; CIRCUIT ARRANGEMENTS FOR ELECTRIC LIGHT SOURCES, IN GENERAL
    • H05B33/00Electroluminescent light sources
    • H05B33/12Light sources with substantially two-dimensional radiating surfaces
    • H05B33/14Light sources with substantially two-dimensional radiating surfaces characterised by the chemical or physical composition or the arrangement of the electroluminescent material, or by the simultaneous addition of the electroluminescent material in or onto the light source
    • HELECTRICITY
    • H10SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10KORGANIC ELECTRIC SOLID-STATE DEVICES
    • H10K50/00Organic light-emitting devices
    • H10K50/10OLEDs or polymer light-emitting diodes [PLED]
    • H10K50/11OLEDs or polymer light-emitting diodes [PLED] characterised by the electroluminescent [EL] layers
    • HELECTRICITY
    • H10SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10KORGANIC ELECTRIC SOLID-STATE DEVICES
    • H10K50/00Organic light-emitting devices
    • H10K50/10OLEDs or polymer light-emitting diodes [PLED]
    • H10K50/18Carrier blocking layers
    • HELECTRICITY
    • H10SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10KORGANIC ELECTRIC SOLID-STATE DEVICES
    • H10K50/00Organic light-emitting devices
    • H10K50/10OLEDs or polymer light-emitting diodes [PLED]
    • H10K50/18Carrier blocking layers
    • H10K50/181Electron blocking layers
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K2211/00Chemical nature of organic luminescent or tenebrescent compounds
    • C09K2211/10Non-macromolecular compounds
    • C09K2211/1003Carbocyclic compounds
    • C09K2211/1007Non-condensed systems
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K2211/00Chemical nature of organic luminescent or tenebrescent compounds
    • C09K2211/10Non-macromolecular compounds
    • C09K2211/1003Carbocyclic compounds
    • C09K2211/1011Condensed systems
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K2211/00Chemical nature of organic luminescent or tenebrescent compounds
    • C09K2211/10Non-macromolecular compounds
    • C09K2211/1003Carbocyclic compounds
    • C09K2211/1014Carbocyclic compounds bridged by heteroatoms, e.g. N, P, Si or B
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K2211/00Chemical nature of organic luminescent or tenebrescent compounds
    • C09K2211/10Non-macromolecular compounds
    • C09K2211/1018Heterocyclic compounds
    • C09K2211/1025Heterocyclic compounds characterised by ligands
    • C09K2211/1044Heterocyclic compounds characterised by ligands containing two nitrogen atoms as heteroatoms
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K2211/00Chemical nature of organic luminescent or tenebrescent compounds
    • C09K2211/10Non-macromolecular compounds
    • C09K2211/1018Heterocyclic compounds
    • C09K2211/1025Heterocyclic compounds characterised by ligands
    • C09K2211/1088Heterocyclic compounds characterised by ligands containing oxygen as the only heteroatom
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K2211/00Chemical nature of organic luminescent or tenebrescent compounds
    • C09K2211/10Non-macromolecular compounds
    • C09K2211/1018Heterocyclic compounds
    • C09K2211/1025Heterocyclic compounds characterised by ligands
    • C09K2211/1096Heterocyclic compounds characterised by ligands containing other heteroatoms
    • HELECTRICITY
    • H10SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10KORGANIC ELECTRIC SOLID-STATE DEVICES
    • H10K2101/00Properties of the organic materials covered by group H10K85/00
    • H10K2101/10Triplet emission
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02EREDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E10/00Energy generation through renewable energy sources
    • Y02E10/50Photovoltaic [PV] energy
    • Y02E10/549Organic PV cells

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Physics & Mathematics (AREA)
  • Optics & Photonics (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Molecular Biology (AREA)
  • General Health & Medical Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Biochemistry (AREA)
  • Spectroscopy & Molecular Physics (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Manufacturing & Machinery (AREA)
  • Electroluminescent Light Sources (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Photovoltaic Devices (AREA)
JP2013503205A 2010-04-06 2011-04-05 置換カルバゾール誘導体および有機エレクトロニクスにおけるその使用 Active JP5931051B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
EP10159162 2010-04-06
EP10159162.6 2010-04-06
PCT/IB2011/051453 WO2011125020A1 (fr) 2010-04-06 2011-04-05 Dérivés de carbazole substitués et leur utilisation en électronique organique

Publications (3)

Publication Number Publication Date
JP2013528929A JP2013528929A (ja) 2013-07-11
JP2013528929A5 JP2013528929A5 (fr) 2014-05-22
JP5931051B2 true JP5931051B2 (ja) 2016-06-08

Family

ID=44762071

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2013503205A Active JP5931051B2 (ja) 2010-04-06 2011-04-05 置換カルバゾール誘導体および有機エレクトロニクスにおけるその使用

Country Status (5)

Country Link
EP (1) EP2556075B1 (fr)
JP (1) JP5931051B2 (fr)
KR (1) KR102018920B1 (fr)
CN (1) CN102933582A (fr)
WO (1) WO2011125020A1 (fr)

Families Citing this family (30)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103517964B (zh) 2011-05-10 2018-05-18 巴斯夫欧洲公司 新型颜色转换器
KR102023787B1 (ko) 2011-06-10 2019-09-20 바스프 에스이 신규 색 변환기
US8652656B2 (en) * 2011-11-14 2014-02-18 Universal Display Corporation Triphenylene silane hosts
CN103204846A (zh) * 2012-01-12 2013-07-17 昱镭光电科技股份有限公司 咔唑衍生物及其有机电激发光装置及制造方法
KR102054229B1 (ko) * 2012-01-13 2019-12-11 덕산네오룩스 주식회사 유기전기 소자용 화합물, 이를 이용한 유기전기소자 및 그 전자 장치
WO2013179645A1 (fr) * 2012-05-30 2013-12-05 出光興産株式会社 Matériau d'élément électroluminescent organique, et élément électroluminescent organique l'utilisant
CN102827196B (zh) * 2012-09-12 2015-06-03 山西大学 一种含硼吲哚[3,2-b]咔唑衍生物及其制备方法和应用
JP6310850B2 (ja) * 2012-09-28 2018-04-11 新日鉄住金化学株式会社 有機電界発光素子用材料及びこれを用いた有機電界発光素子
TWI599570B (zh) * 2012-09-28 2017-09-21 新日鐵住金化學股份有限公司 Compounds for organic electroluminescent devices and organic electroluminescent devices
KR101547623B1 (ko) * 2012-10-24 2015-08-26 주식회사 두산 유기 전계 발광 소자
KR101684979B1 (ko) * 2012-12-31 2016-12-09 제일모직 주식회사 유기광전자소자 및 이를 포함하는 표시장치
JP6389459B2 (ja) * 2013-06-14 2018-09-12 保土谷化学工業株式会社 ジカルバゾール誘導体及び有機エレクトロルミネッセンス素子
KR101759238B1 (ko) 2013-09-05 2017-07-18 제일모직 주식회사 유기 광전자 소자용 화합물, 이를 포함하는 유기 광전자 소자 및 상기 유기 광전자 소자를 포함하는 표시장치
CN103601747B (zh) * 2013-11-27 2015-09-30 山西大学 一种基于吲哚[3,2-b]咔唑的芳基硼化合物及其制备和应用
CN104046351B (zh) * 2014-04-29 2016-11-16 中山大学 具有余辉发光性能的有机发光材料及其合成方法和应用
US10749118B2 (en) 2014-06-26 2020-08-18 Samsung Display Co., Ltd. Heterocyclic compound and organic light-emitting device including the same
TWI666803B (zh) * 2014-09-17 2019-07-21 日商日鐵化學材料股份有限公司 有機電場發光元件及其製造方法
CN104610329B (zh) * 2015-02-04 2016-11-23 中国科学院长春应用化学研究所 双硼氮桥联联吡啶及用其制备的有机/高分子材料
CN107207522A (zh) * 2015-02-16 2017-09-26 出光兴产株式会社 化合物、有机电致发光元件用材料、有机电致发光元件和电子器件
CN105295010A (zh) * 2015-10-15 2016-02-03 中国科学院长春应用化学研究所 基于双硼氮桥联联吡啶的共轭聚合物及其制备方法与应用
CN105198889A (zh) * 2015-10-23 2015-12-30 西安近代化学研究所 一种6-芳基取代的咪唑并[4,5-c]吲哚并[2,3-a]咔唑衍生物及其制备方法
JP6834400B2 (ja) * 2016-11-22 2021-02-24 ソニー株式会社 撮像素子、積層型撮像素子、撮像装置及び電子装置
CN107337680B (zh) * 2017-07-17 2019-02-22 江苏三月光电科技有限公司 一种以芴为核心的有机化合物及其在oled器件上的应用
CN110272427B (zh) * 2018-03-14 2022-03-29 江苏三月科技股份有限公司 一种以芴为核心的化合物、其制备方法及其在有机电致发光器件上的应用
CN110092789B (zh) * 2019-06-12 2021-10-22 贵州省中国科学院天然产物化学重点实验室(贵州医科大学天然产物化学重点实验室) 一种吲哚并[2,3-b]咔唑衍生物及其应用
CN112250685B (zh) * 2020-11-25 2022-04-19 中钢集团南京新材料研究院有限公司 一种吲哚并[2,3-a]咔唑的制备方法
JP7264182B2 (ja) * 2021-02-03 2023-04-25 ソニーグループ株式会社 撮像素子、積層型撮像素子、撮像装置及び電子装置
CN113957480B (zh) * 2021-11-09 2022-11-22 深圳先进技术研究院 电化学催化二氧化碳还原储能用铜基催化剂、电极、其制备方法及应用
CN113980026B (zh) * 2021-11-25 2024-03-29 上海钥熠电子科技有限公司 咔唑衍生物类胺化合物和包含其的有机电致发光器件
CN114539270B (zh) * 2021-12-09 2024-03-29 上海钥熠电子科技有限公司 含有咔唑衍生物的化合物及其在有机电致发光器件中的应用

Family Cites Families (19)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3835842A1 (de) * 1988-10-21 1990-04-26 Goedecke Ag Indolocarbazol-derivate, verfahren zu deren herstellung und deren verwendung als arzneimittel
US5952115A (en) * 1997-10-02 1999-09-14 Xerox Corporation Electroluminescent devices
WO2005077956A1 (fr) * 2004-02-16 2005-08-25 Ihara Chemical Industry Co., Ltd. Sym-triindole substituee
WO2006033538A1 (fr) * 2004-09-20 2006-03-30 Lg Chem. Ltd. Derive de carbazole et dispositif electroluminescent organique utilisant ledit derive
US7173140B2 (en) * 2004-12-14 2007-02-06 Xerox Corporation Process to form compound with indolocarbazole moieties
US8217181B2 (en) * 2004-12-30 2012-07-10 E. I. Du Pont De Nemours And Company Dihalogen indolocarbazole monomers and poly (indolocarbazoles)
KR101082258B1 (ko) * 2005-12-01 2011-11-09 신닛테츠가가쿠 가부시키가이샤 유기 전계 발광소자용 화합물 및 유기 전계 발광소자
US20070224446A1 (en) * 2006-03-24 2007-09-27 Idemitsu Kosan Co., Ltd. Material for organic electroluminescence device and organic electroluminescence device using the same
JP5081821B2 (ja) * 2006-06-02 2012-11-28 出光興産株式会社 有機エレクトロルミネッセンス素子用材料及びそれを用いた有機エレクトロルミネッセンス素子
WO2008056746A1 (fr) * 2006-11-09 2008-05-15 Nippon Steel Chemical Co., Ltd. Composé pour un dispositif électroluminescent organique et dispositif électroluminescent organique
CN101688114B (zh) * 2007-07-05 2014-07-16 巴斯夫欧洲公司 包含至少一种选自二甲硅烷基咔唑、二甲硅烷基二苯并呋喃、二甲硅烷基二苯并噻吩、二甲硅烷基二苯并磷杂环戊二烯、二甲硅烷基二苯并噻吩s-氧化物和二甲硅烷基二苯并噻吩s,s-二氧化物的二甲硅烷基化合物的有机发光二极管
KR101082144B1 (ko) * 2008-05-08 2011-11-09 신닛테츠가가쿠 가부시키가이샤 유기 전계 발광 소자용 화합물 및 유기 전계 발광 소자
EP2301921A4 (fr) * 2008-06-05 2012-06-20 Idemitsu Kosan Co Composé polycyclique et dispositif électroluminescent organique l'utilisant
EP2145936A3 (fr) * 2008-07-14 2010-03-17 Gracel Display Inc. Dérivés de fluorène et pyrène et dispositif électroluminescent organique les utilisant
KR101511072B1 (ko) * 2009-03-20 2015-04-10 롬엔드하스전자재료코리아유한회사 신규한 유기 발광 화합물 및 이를 포함하는 유기 전계 발광소자
KR20100118700A (ko) * 2009-04-29 2010-11-08 다우어드밴스드디스플레이머티리얼 유한회사 신규한 유기 발광 화합물 및 이를 채용하고 있는 유기 전계 발광 소자
JP5711220B2 (ja) * 2009-05-15 2015-04-30 チェイル インダストリーズ インコーポレイテッド 有機光電素子用化合物およびこれを含む有機光電素子
JP5457907B2 (ja) * 2009-08-31 2014-04-02 ユー・ディー・シー アイルランド リミテッド 有機電界発光素子
KR101324788B1 (ko) * 2009-12-31 2013-10-31 (주)씨에스엘쏠라 유기 광소자 및 이를 위한 유기 광합물

Also Published As

Publication number Publication date
CN102933582A (zh) 2013-02-13
EP2556075B1 (fr) 2019-02-27
EP2556075A4 (fr) 2013-10-02
KR20130094183A (ko) 2013-08-23
KR102018920B1 (ko) 2019-09-05
JP2013528929A (ja) 2013-07-11
EP2556075A1 (fr) 2013-02-13
WO2011125020A1 (fr) 2011-10-13

Similar Documents

Publication Publication Date Title
JP5931051B2 (ja) 置換カルバゾール誘導体および有機エレクトロニクスにおけるその使用
US11031559B2 (en) Phenoxasiline based compounds for electronic application
US8637857B2 (en) Substituted carbazole derivatives and use thereof in organic electronics
JP5808252B2 (ja) カルバゾール、ジベンゾフラン、ジベンゾチオフェンおよびジベンゾホスホールから選択されたシリル置換およびヘテロ原子置換された化合物および該化合物の有機エレクトロニクスへの使用
JP5661635B2 (ja) 縮合環系で置換されたシロール及び有機エレクトロニクスにおけるその使用
JP6072681B2 (ja) 窒素結合5員環複素環により置換されたジベンゾフラン及びジベンゾチオフェン及び有機エレクトロニクスにおけるそれらの使用
JP5804703B2 (ja) ジシリルカルバゾール、ジシリルジベンゾフラン、ジシリルジベンゾチオフェン、ジシリルジベンゾホスホール、ジシリルジベンゾチオフェンs−オキシドおよびジシリルジベンゾチオフェンs,s−ジオキシドから選択される少なくとも1つのジシリル化合物を含む有機発光ダイオード
JP5675349B2 (ja) カルベン遷移金属錯体発光体、ならびにジシリルカルバゾール、ジシリルジベンゾフラン、ジシリルジベンゾチオフェン、ジシリルジベンゾホスホール、ジシリルジベンゾチオフェンs−オキシドおよびジシリルジベンゾチオフェンs,s−ジオキシドから選択される少なくとも1つの化合物を含む有機発光ダイオード
US9067919B2 (en) Use of dibenzofurans and dibenzothiophenes substituted by nitrogen-bonded five-membered heterocyclic rings in organic electronics

Legal Events

Date Code Title Description
A521 Request for written amendment filed

Free format text: JAPANESE INTERMEDIATE CODE: A523

Effective date: 20140402

A621 Written request for application examination

Free format text: JAPANESE INTERMEDIATE CODE: A621

Effective date: 20140402

A131 Notification of reasons for refusal

Free format text: JAPANESE INTERMEDIATE CODE: A131

Effective date: 20150302

A601 Written request for extension of time

Free format text: JAPANESE INTERMEDIATE CODE: A601

Effective date: 20150601

A601 Written request for extension of time

Free format text: JAPANESE INTERMEDIATE CODE: A601

Effective date: 20150618

A521 Request for written amendment filed

Free format text: JAPANESE INTERMEDIATE CODE: A523

Effective date: 20150731

RD03 Notification of appointment of power of attorney

Free format text: JAPANESE INTERMEDIATE CODE: A7423

Effective date: 20150910

A131 Notification of reasons for refusal

Free format text: JAPANESE INTERMEDIATE CODE: A131

Effective date: 20151005

A521 Request for written amendment filed

Free format text: JAPANESE INTERMEDIATE CODE: A523

Effective date: 20151014

TRDD Decision of grant or rejection written
A01 Written decision to grant a patent or to grant a registration (utility model)

Free format text: JAPANESE INTERMEDIATE CODE: A01

Effective date: 20160328

A61 First payment of annual fees (during grant procedure)

Free format text: JAPANESE INTERMEDIATE CODE: A61

Effective date: 20160426

R150 Certificate of patent or registration of utility model

Ref document number: 5931051

Country of ref document: JP

Free format text: JAPANESE INTERMEDIATE CODE: R150

S111 Request for change of ownership or part of ownership

Free format text: JAPANESE INTERMEDIATE CODE: R313117

R371 Transfer withdrawn

Free format text: JAPANESE INTERMEDIATE CODE: R371

S111 Request for change of ownership or part of ownership

Free format text: JAPANESE INTERMEDIATE CODE: R313117

R360 Written notification for declining of transfer of rights

Free format text: JAPANESE INTERMEDIATE CODE: R360

R360 Written notification for declining of transfer of rights

Free format text: JAPANESE INTERMEDIATE CODE: R360

R371 Transfer withdrawn

Free format text: JAPANESE INTERMEDIATE CODE: R371

S111 Request for change of ownership or part of ownership

Free format text: JAPANESE INTERMEDIATE CODE: R313117

R350 Written notification of registration of transfer

Free format text: JAPANESE INTERMEDIATE CODE: R350

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250